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RecruitingAccepts healthy volunteersPhase 2/Phase 3

Nonopioid Analgesia After Labral Surgery

Henry Ford Health System · NCT03825809

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 2, Phase 3
Target enrollment
100
US sites recruiting
1
Study start
January 22, 2019
Record last updated
January 31, 2019

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen

Being studied: Celecoxib; Hydrocodone-Acetaminophen; Ketorolac; Gabapentin; Acetaminophen; Diazepam

Conditions: Narcotic Use

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Eligibility Criteria

Inclusion Criteria

  • All adult patients over age 18 and scheduled for a primary or revision labral surgery

Exclusion Criteria

  • Exclusion criteria will include patients with a medical history of known allergies or intolerance to allergies or intolerance to Celebrex, Tylenol, Neurontin, dexamethasone, tramadol, substantial alcohol or drug abuse, and pregnancy, history of narcotics within 6 months of surgery, renal impairment, peptic ulcer disease, GI bleeding. Secondary exclusion criterion is an intact rotator cuff

Recruiting US locations

  • Henry Ford Health System

    Detroit, MI 48202

    Site contact: Toufic R Jildeh, MD

Study contacts (from the official record)

  • Toufic R Jildeh, MD · 517-230-8511 · tjildeh1@hfhs.org
All healthy volunteers studies in Michigan →
Nonopioid Analgesia After Labral Surgery (NCT03825809) | Bored Studies